BBa_K180020BBa_K180020 Version 1 (Component)Rock-paper-scissors - Scissors secondary plasmid [las pR, LacI generator]
BBa_K180013BBa_K180013 Version 1 (Component)Rock-paper-scissors - Rock secondary plasmid [rhl pR, LacI generator]
BBa_K2044010BBa_K2044010 Version 1 (Component)Based on our project, <5,7> is the direct pathway from Site No.5to Site No.7 in the map we design.
BBa_K737000BBa_K737000 Version 1 (Component)We got this part from the mutant of E.coli strain K12, DH5α,using PCR with the primers we desig
BBa_I23000BBa_I23000 Version 1 (Component)RBS Scaffold with mCherry reporter
BBa_K1106000BBa_K1106000 Version 1 (Component)mRFP generator under hybrid promoter: HSL-LuxR activated, P22 C2 repressed
BBa_I9005BBa_I9005 Version 1 (Component)nor_input (tp901-cI) B0034.C0075
BBa_K091230BBa_K091230 Version 1 (Component)cI promoter+RBS+RFP+TT
BBa_I744111BBa_I744111 Version 1 (Component)Tc-driven cI (lambda) generator
BBa_K2044006BBa_K2044006 Version 1 (Component)Based on our project,<3,6> is the direct pathway from Site No.3 to Site No.6 in the map we design.
BBa_K2044004BBa_K2044004 Version 1 (Component)Based on our project, <2,4> is the direct pathway from Site No.2 to Site No.4 in the map we design.
BBa_K2044009BBa_K2044009 Version 1 (Component)Based on our project, <4,8> is the direct pathway from Site No.4 to Site No.8 in the map we design.
BBa_K2044014BBa_K2044014 Version 1 (Component)Based on our project, <1,4> is the direct pathway from Site No.1 to Site No.4 in the map we design.
BBa_K2044007BBa_K2044007 Version 1 (Component)Based on our project, <4,5> is the direct pathway from Site No.4 to Site No.5 in the map we design.
BBa_K2044013BBa_K2044013 Version 1 (Component)Based on our project,<7,8> is the direct pathway from Site No.7 to Site No.8 in the map we design.
BBa_K2044008BBa_K2044008 Version 1 (Component)Based on our project, <4,6> is the direct pathway from Site No.4 to Site No.6 in the map we design.
BBa_K2044003BBa_K2044003 Version 1 (Component)Based on our project, <2,3> is the direct pathway from Site No.2 to Site No.3 in the map we design.
BBa_K2044002BBa_K2044002 Version 1 (Component)Based on our project, <2,1> is the direct pathway from Site No.2 to Site No.1 in the map we design.
BBa_K2044005BBa_K2044005 Version 1 (Component)Based on our project, <2,6> is the direct pathway from Site No.2 to Site No.6 in the map we design.
BBa_K2044012BBa_K2044012 Version 1 (Component)Based on our project, <6,8> is the direct pathway from Site No.6 to Site No.8 in the map we design.
BBa_K2044011BBa_K2044011 Version 1 (Component)Based on our project,<6,4> is the direct pathway from Site No.6 to Site No.4 in the map we design.
BBa_K1520017BBa_K1520017 Version 1 (Component)Pcons2-rbs-luxR-Ter-Prlux-rbs-lacI-Ter-Plac-rbs-rfp-Ter
BBa_M50050BBa_M50050 Version 1 (Component)IPTG-Inducible LuxS Expression in E. coli for Controlling Growth Rates
BBa_K737001BBa_K737001 Version 1 (Component)We got this part from the mutant of E.coli strain K12, DH5α,using PCR with the primers we desig
SEGASEGA_collection Version 1 (Collection)In the Standardized Genome Architecture (SEGA), genomic integration of DNA fragments is enabled by λ-Red recombineering and so-called landing pads that are a common concept in synthetic biology and typically contain features that i) enable insertion of additional genetic elements and ii) provide well-characterized functional parts such as promoters and genes, and iii) provides insulation against genome context-dependent effects. The SEGA landing pads allow for reusable homology regions and time-efficient construction of parallel genetic designs with a minimal number of reagents and handling steps. SEGA bricks, typically synthetic DNA or PCR fragments, are integrated on the genome simply by combining the two reagents (i.e. competent cells and DNA), followed by incubation steps, and successful recombinants are identified by visual inspection on agar plates. The design of the SEGA standard was heavily influenced by the Standard European Vector Architecture (SEVA). SEGA landing pads typically hosts two major genetic “control elements” that influence gene expression on the transcriptional (C1), and translational (C2) level. Furthermore, landing pads contain gadgets such as selection and counterselection markers.
BBa_K327015BBa_K327015 Version 1 (Component)Lux activated, C1lam repressed switch
BBa_J24822BBa_J24822 Version 1 (Component)Same as J24819 but with the error at the luc-terminator junction fixed
BBa_I10200BBa_I10200 Version 1 (Component)434 cI repressor protein generator
BBa_K1647000BBa_K1647000 Version 1 (Component)CI operator site with GFP
BBa_K180015BBa_K180015 Version 1 (Component)Paper - Primary plasmid (part 2) [tac pR, GFP and RhlI generator]
BBa_K077125BBa_K077125 Version 1 (Component)Test construct for HSL/LuxR or LasR promotors, with LacZalpha output
BBa_J13101BBa_J13101 Version 1 (Component)LacI repressed lambda CI generator
PL GFPBBa_K193000 Version 1 (Component)GFP reporter regulated by CI.
BBa_K1767010BBa_K1767010 Version 1 (Component)P(Lac)IQ RBS LuxR ter ter luxpR RBS eyfp ter ter
BBa_K132019BBa_K132019 Version 1 (Component)rhlR+terminator+Prhl+luxI+kanR-LVA+lacI+PL+kanR-LVA+aiiA+terminator
BBa_K1053300BBa_K1053300 Version 1 (Component)PLtetO-1-RBS-cI-DT
BBa_K145008BBa_K145008 Version 1 (Component)LuxR generator
BBa_K750004BBa_K750004 Version 1 (Component)LuxI expression device activated by arabinose(Regulated by RBS of 0.07 strength)
BBa_J23039BBa_J23039 Version 1 (Component)[TetR]+[rbs][LuxI][dblTerm] "Constitutive luxI"
BBa_K909004BBa_K909004 Version 1 (Component)cI with strong ribosomal binding site
BBa_I719022BBa_I719022 Version 1 (Component)cI promoter with GFP reporter
BBa_J10064BBa_J10064 Version 1 (Component)Lux Operon Vibrio fischeri from part K325909
BBa_K1141000BBa_K1141000 Version 1 (Component)Plac-RBS-mCherry-double terminator (IPTG-inducible)
BBa_K1073017BBa_K1073017 Version 1 (Component)Lux I + LVA with RBS and double terminator
BBa_S03968BBa_S03968 Version 1 (Component)RBS-LuxS
BBa_K1725346BBa_K1725346 Version 1 (Component)<i>luxC</i> with optimised RBS for expression in <i>E. coli</i>
BBa_K1725349BBa_K1725349 Version 1 (Component)<i>luxE</i> with optimised RBS for expression in <i>E. coli</i>
BBa_K1725347BBa_K1725347 Version 1 (Component)<i>luxG</i> with optimised RBS for expression in <i>E. coli</i>
BBa_K1725348BBa_K1725348 Version 1 (Component)<i>luxD</i> with optimised RBS for expression in <i>E. coli</i>
BBa_K1725345BBa_K1725345 Version 1 (Component)<i>luxB</i> with optimised RBS for expression in <i>E. coli</i>